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Moderate recall: A hazard has been identified, with no injuries reported yet. Follow the steps below.

SOMERSET THERAPEUTICS LLC 2025-12-24 Health moderate FDA
Health · FDA · Recall #FDA-D-0238-2026

Cisatracurium Besylate Injection USP, 20 mg/10 mL*,(2 mg/mL), 10 x 10 mL Multiple-dose… Recall

Issued December 24, 2025 · SOMERSET THERAPEUTICS LLC

In December 2025, SOMERSET THERAPEUTICS LLC recalled the Cisatracurium Besylate Injection USP, 20 mg/10 mL*,(2 mg/mL), 10 x 10 mL Multiple-dose…, a moderate health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Subpotent product:out of specification assay results observed during long term stability testing.

What you should do

  1. 1 Stop using Cisatracurium Besylate Injection USP, 20 mg/10 mL*,(2 mg/mL), 10 x 10 mL Multiple-dose… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact SOMERSET THERAPEUTICS LLC to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
SOMERSET THERAPEUTICS LLC
Category
Health
Recall date
December 24, 2025
Units affected
Not reported
Sold at
Nationwide in the USA
Recall number
FDA-D-0238-2026
Made in
United States
Issuing agency
FDA

In context

  • SOMERSET THERAPEUTICS LLC has 2 recalls in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 691st Health recall we've logged in 2025.
Read the official FDA notice

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